The present invention relates to the field of focused ultrasound, and more precisely, to treatment by focused ultrasound.
Focused ultrasound makes it possible to treat deep tissues without direct access to these tissues. A focused ultrasound beam originating from a power transducer is concentrated towards a focus which is positioned on the target. This results in a double thermal and cavitation phenomenon. The tissue effect depends on the application of the ultrasound energy. Under certain conditions (moderate acoustic intensity), a thermal effect is obtained, under others (strong acoustic intensity), the cavitation effect predominates. The choice of treatment parameters (acoustic intensity and frequency, duration of firing, duration of pauses between the firings, spacing between the firings etc.) is made in order to avoid burning in the intermediate tissues, i.e., situated between the ultrasound source and the target. The designation “acoustic axis” of the transducer is given to a line joining the center of the transducer, or its center of symmetry (if it exists) and the focus. In the case of a plane transducer and electronic focusing, the acoustic axis is the axis perpendicular to the transducer plane, and passing through the focus; the acoustic axis can also generally be defined as passing through the focus and directed following the mean direction of ultrasound propagation.
The effect of each ultrasound pulse is generally limited to a small spatial zone, in which the intensity of the ultrasound field is strongest, and which is situated around the focus. The focal zone will typically have the shape of a cylinder 1.5 mm in diameter in a plane perpendicular to the acoustic propagation direction and 10 mm in length in the acoustic propagation direction.
This technique is particularly useful when the treatment must be precise, for example when the zone to be treated is close to sensitive organs to be preserved. This is the case for example with treatment of the prostate, in which the external sphincter must not be touched for fear of causing incontinence in the patient.
It has therefore been proposed to combine in one therapy appliance a treatment transducer and an imaging transducer; in fact ultrasound marking is useful because it is simple, inexpensive and emits no ionizing radiation. The imaging transducer is used, as its name indicates, to obtain an image of the zone to be treated. The treatment transducer, or power transducer, is used for the emission of the ultrasound intended for the treatment. From the quantitative point of view, the average power range for the imaging transducer is typically of the order of 0.1 to 1 W, while the average power range for the treatment transducer is typically of the order of 5 to 100 W. Moreover, the ultrasound pulses emitted for the imaging have a typical duration of 0.1 μs to 1 μs, whilst the therapy pulses last from 0.1 s to 20 s. In order to make it possible to visualize a volume containing the target, a displacement of the imaging transducer scanning plane can be provided.
Ultrasound therapy appliances combined with ultrasound scanning have been described. In EP-A-0 148 653, EP-A-0 162 735 and U.S. Pat. No. 5,431,621, an imaging transducer is accommodated in the center of a cap serving as treatment transducer; this cap has axial symmetry. The scanning plane of the imaging transducer contains the acoustic axis of the treatment transducer. The ultrasound imaging transducer can turn on its axis, but this is not the case with the treatment transducer. It is proposed in these documents to use the appliance to destroy renal calculi by shock waves or to treat tumors by hyperthermia.
WO-A-92 15253 describes a bevelled endorectal probe. The probe is mounted in rotation on a support and in translation along its longitudinal axis. The treatment transducer is fixed with respect to the probe body. The probe has an imaging transducer, which is fixed or mobile with respect to the treatment transducer. In all cases, the imaging transducer's scanning plane contains the focus of the treatment transducer.
EP-A-0-714 266 describes an endorectal probe suitable for treatment of the prostate. The probe comprises retractable therapy and imaging transducers. In the “imaging” position, the second transducer scans a plane containing the acoustic axis of treatment. The scanning plane is variable, as it can pivot about this axis. The treatment transducer does not turn about its acoustic axis, but about an axis which is parallel to the axis of the endorectal probe.
WO-A-89 07909 discloses, in
WO-A-95 02994 discloses, in
These different appliances of the state of the art are only slightly or not at all suitable for the treatment of organs from outside the body, and for example for focused ultrasound treatment of the thyroid. A need therefore exists for an appliance which can treat organs such as the thyroid, by focused ultrasound, simply, with precision, and effectively.
In one embodiment, the invention provides a focused ultrasound treatment probe, which is suitable for treatment of different organs from outside the body. The probe has a probe body which is mounted in rotation on a support. The probe body comprises an elongated treatment transducer, the acoustic axis of which is substantially the same as the axis of rotation of the probe body. The probe body also has an imaging transducer, the scanning plane of which contains the acoustic axis of the treatment transducer.
The fact that the transducer is elongated allows high-precision emission: the cone formed by the acoustic waves is asymmetrical and has an angle at the apex—at the focus—which is less open in the transverse direction of the transducer than in the longitudinal direction of the transducer. It is easier to avoid the organs close to the target. The fact that the acoustic axis is substantially the same as the axis of rotation of the probe body ensures that the probe body can turn about the axis of rotation, without however the position of the focus with respect to the target moving. It is then possible to displace the probe body in rotation, for imaging or treatment, without however displacing the transducers.
As the scanning plane—or imaging plane—of the imaging transducer contains the acoustic axis and therefore also contains the axis of rotation of the probe body, the target being situated at the focus of the treatment transducer remains in the imaging plane during rotation of the probe body.
The invention moreover proposes that the treatment transducer be mounted so that it is mobile in the probe body. It is in particular possible for the treatment transducer to be mounted in rotation in the probe body about an axis perpendicular to the axis of rotation.
This configuration makes it possible for the imaging transducer to also be mounted so that it is mobile in the probe body. It can in particular be mounted in translation in the probe body, preferably following a direction parallel to the axis of rotation.
In one embodiment, the treatment transducer has an aspect ratio greater than 1.2. It is also advantageous for the treatment transducer to have an aspect ratio smaller than 2.5.
Preferably, the imaging transducer is an array carrying out a linear scan. It is then advantageous for the axis of this transducer to be parallel to the longitudinal direction of the treatment transducer. The imaging transducer can in particular be integrated into the treatment transducer.
In another embodiment, the probe has a support on which the probe is mounted in rotation, the support displacing the probe in translation in a plane perpendicular to the axis of rotation. In this case, the support can moreover displace the probe in translation following the direction of the axis of rotation.
The support can also have a ball-and-socket joint for orientation of the probe. Another solution is for the support to have an arch along which the probe moves; it is then advantageous for the radius of the arch to be substantially equal to the distance between the arch and the focus of the treatment transducer.
A subject of the invention is therefore a focused ultrasound treatment probe, comprising a probe body mounted in rotation about an axis, an elongated treatment transducer, with an acoustic axis of focused ultrasound emission substantially the same as the axis of rotation of the probe body, an imaging transducer the imaging plane of which contains the acoustic axis of the treatment transducer.
According to one embodiment, the treatment transducer is mounted so that it is mobile in the probe body.
According to another embodiment, the treatment transducer is mounted in rotation in the probe body preferably about an axis perpendicular to the axis of rotation.
According to yet another embodiment, the imaging transducer is mounted so that it is mobile in the probe body.
According to yet another embodiment, the imaging transducer is mounted in translation in the probe body, preferably following a direction parallel to the axis of rotation.
It can also be provided that the treatment transducer has an aspect ratio greater than 2.2. It can advantageously be provided that the treatment transducer has an aspect ratio smaller than 2.5.
According to one embodiment, the imaging transducer is an array carrying out a linear scan.
According to another embodiment, the imaging transducer axis is parallel to the longitudinal direction of the treatment transducer.
According to yet another embodiment, the imaging transducer is integrated in the treatment transducer.
According to yet another embodiment, the probe has a support on which the probe is mounted in rotation, the support displacing the probe in translation in a plane perpendicular to the axis of rotation.
It can moreover be provided that the support moreover displaces the probe in translation following the direction of the axis of rotation.
According to one embodiment, the support has a ball-and-socket joint for orientation of the probe.
According to yet another embodiment, the support has an arch along which the probe moves.
According to another embodiment, the radius of the arch is substantially equal to the distance between the arch and the focus of the treatment transducer.
Other characteristics and advantages of the invention will become apparent on reading the following description of embodiments of the invention, given by way of example and with reference to the attached drawings.
In this written description, the use of the disjunctive is intended to include the conjunctive. The use of definite or indefinite articles is not intended to indicate cardinality. In particular, a reference to “the” object or thing or “an” object or “a” thing is intended to also describe a plurality of such objects or things.
Moreover, a mask is provided, the function of which is explained with reference to
As shown in the figure, the axis of rotation 8 of the probe body passes substantially through the focus, the treatment transducer extends in a plane which is substantially perpendicular to the axis of rotation 8; thus the acoustic axis of the transducer is substantially the same as the axis of rotation of the probe. In practice, it is advantageous for the acoustic axis to be exactly the same as the axis of rotation of the probe—allowing for any mechanical clearances. Nevertheless a displacement can be allowed between the acoustic axis and the axis of rotation, to the extent that the displacement of the focal point during the rotation of the probe body about the axis of rotation remains limited, and typically remains smaller than the transverse dimension of the focal zone. In terms of distance, the distance between the acoustic axis and the probe axis is advantageously less than 1 mm, throughout the zone extending between the focus and the treatment transducer; in terms of angles, an angle can be allowed between the direction of the acoustic axis and the direction of the axis of rotation of up to 15°.
The figure does not show the recurrent laryngeal nerves which control the vocal chords and pass behind the two lobes of the thyroid gland. These nerves are protected during treatment, to the extent that they are situated behind the zone aimed at. The esophagus, which is situated behind the trachea, is also not shown.
In order to reinforce the safety of the treatment, it is also possible to use the probe described with a tracheal probe, which is installed in the patient's trachea during treatments. For example the probe can be an NIM Response® nerve integrity monitor, marketed by the company Xomed. It comprises electrodes placed in proximity to the recurrent laryngeal nerves, which thus make it possible to detect any alterations to these nerves due to the ultrasound energy emitted during the treatment.
It is also possible to use a tracheal probe comprising a balloon, positioned facing the thyroid and through which cold water circulates, which makes it possible to cool the trachea down and thus to protect it from any thermal damage. A probe combining electrodes and a cold circulation can also be used.
In the probe's imaging position, the imaging plane contains the acoustic axis, and therefore also contains the axis of rotation of the probe body. It is therefore possible, during the rotation of the probe body, to obtain in a continuous fashion, the image of the zone of the organ to be treated which is covered by the target. It is also possible to mark on the ultrasonographic image the position of the focus or even the position or extent of the lesions which will be made by the treatment transducer.
In order to return to the treatment position represented in
In either case, the two plates allow displacement of the probe, perpendicularly to the acoustic axis. In fact, each acoustic pulse causes necrosis of the tissue in a small volume. In order to treat a complete target, the head is thus displaced between the firings, by means of the plates.
It is also advantageous to orient the front part of the probe substantially perpendicular to the skin. This makes it possible to keep a constant depth from one displacement of the head to another. The orientation is possible by means of the ball-and-socket joint in
The probe described has the following advantages. First it ensures precise marking. In fact, the treatment transducer is combined with an imaging transducer, procuring a very fine image and capable of visualizing the whole target. To the extent that the relative positions of the treatment transducer and of the imaging transducer can be determined precisely—in both examples—the images obtained by means of the imaging transducer are in a known and precise spatial relationship with the focal zone of the treatment transducer; the effect of the ultrasound is produced well in the zone visualized by the imaging transducer. The rotation of the probe body about an axis which is the same as the acoustic axis of the treatment transducer and which is contained in the imaging plane ensures high precision, even during displacements of the probe.
The probe also ensures safe treatment, in particular in the case of treatments of the thyroid. The recurrent laryngeal nerves are protected by the two lobes of the thyroid gland. The depth positioning of the focal point, by appropriate inflation of the balloon, ensures high precision depth treatment. The trachea is protected by the positioning of the probe body. The esophagus is situated behind the trachea and protected by the latter. The high volume of blood flow in the carotid protects it from the thermal effects of the ultrasound. As explained above, the elongated shape of the treatment transducer makes it possible to preserve the tissues, by using an ultrasound beam in the form of a flattened cone.
The probe also ensures effective treatment. In order to obtain a treatment effect, for example by coagulation of the tissue in the focal zone, the ultrasound waves must be sufficiently concentrated. For this purpose, the diameter of the transducer is generally allowed to be equal to its focal length. Moreover, the power is a function of the emissive surface. The elongated shape of the transducer makes it possible to satisfy the requirement relating to the diameter of the transducer, without reducing the emissive surface.
The probe is also simple to use. In fact, it can easily be adapted to all patients—the contact area of the probe—the projection onto the patient following the acoustic axis, or the probe's contact zone with the patient is minimal, and corresponds substantially to the size of the therapy transducer.
An example of the probe's functioning sequence is now described, with reference to
At step 82, the operator starts by indicating which side of the patient is treated—right or left. The longitudinal orientation of the probe depends on the side to be treated, as shown in
At step 84, the probe is applied to the patient and oriented in the longitudinal axis of the patient. At this step, the transducer, its acoustic beam and the future lesion can be symbolized on the screen. The practitioner marks on the image the extreme positions “head” and “feet”, which correspond to the cephalo-caudal extension of the target. This marking defines a series of “sections” or successive treatment planes, which are oriented transversally with respect to the patient. The practitioner also marks the position of the skin, for subsequent calculation of the power to be delivered during the firings. This step makes it possible to determine the successive positions of the probe, following the longitudinal direction of the patient. The distance between the “sections” is a function of the size of the zone surrounding the focus in which the tissues are treated. A distance between 10 and 30 mm is suitable.
At step 86, the probe is then displaced towards the first section, which is the position marked “head”. The probe can then be oriented in the transverse axis of the patient. To this end, the transducer, its acoustic beam as it will be during treatment, i.e. when the probe is oriented longitudinally, and the future lesion are symbolized on the screen. The operator can mark the lesions to be treated in the first section.
The operator then displaces the probe towards the second section, in the caudal direction. He follows the same procedure as for the first section, marking the skin and lesions to be treated in this second section. The probe is then displaced towards the following sections, carrying out the marking each time.
At the end of these steps 82 to 86, the contours of the target are determined, and in each section the limits chosen by the operator for the ultrasound treatment are known. A different procedure can of course be followed, for example reversing the scanning directions and using “vertical sections”. However the marking of the contours of the target on the horizontal sections makes it easier to avoid the structures to be preserved, such as the trachea, or the nerves, because these can easily be seen on the transverse sections through the neck. During steps 84 and 86, it is possible to turn the probe, in order to vary the direction of the imaging plane, as explained in detail above.
At step 88, the probe is then switched to firing mode; this can consist of passing from the position in
By way of example, possible treatment parameters are now given, in the case of the thyroid.
The following notations are used:
f excitation frequency of the transducer
Pref E reference power of the transducer in W: this is the electrical power to be supplied for the transducer to generate the intensity required at the focus in order to obtain coagulation necrosis of the tissues in the focal zone;
η electro-acoustic yield of the transducer: ratio between the acoustic power supplied by the transducer and the electric power used;
Pref A reference power of the transducer in W: this is the electrical power which must be supplied by the transducer in order to obtain coagulation necrosis of the tissues in the focal zone; it is defined by Pref A=Pref E*η
Dfoc focal length of the transducer. Short focal lengths will be preferable for thin patients;
Φtot diameter of the transducer, or dimension of the transducer according to its longitudinal direction;
Φtrunc truncated diameter of the transducer or dimension of the transducer according to its transverse direction;
The latter two parameters can be expressed as a function of “the aperture” which is the ratio between the large diameter and the focal length. N=Φtot/Dfoc and the truncation parameter R=Φtrunc/Φtot which is the inverse of the aspect ratio discussed above.
It is also noted that:
DL spacing between the points in the longitudinal direction;
DT spacing between the points in the transverse direction;
Ton duration of each pulse;
Toff interval between each pulse.
The power can be calculated by compensating for the absorption of the tissues by an increase in the power according to the formula:
P=Pref*exp(2*α*1*Dep/10)
where:
α, absorption coefficient of the tissues in Np/cm/MHz. For HIFU treatments, a value (0.06 to 0.08) will be used which is higher than those given by various bibliographical sources, which can be used in ultrasonography (typically 0.04 to 0.05).
Dep thickness of the tissues crossed in mm
Dep is a function of the distance to the skin and the focal length,
Dep=Dfoc−S with:
SDistance from the transducer to the skin.
It has been shown experimentally that the following parameters are particularly suitable for the treatment of thyroid nodules in humans. The minimum and maximum permitted values are designated minn and maxx, the recommended value range limits min and max, and Typ is a typical value considered by way of example.
These values allow treatment in one session of a unit/total duration of approximately 15 minutes. It is found, over a period of several weeks after the treatment, that the nodules disappear, the tissue treated being replaced by a fibrosis.
Of course, the present invention is not limited to the examples and embodiments described and represented, but it is capable of a number of variants accessible to a person skilled in the art. It would thus be possible to use other elongated shapes of treatment transducers. The kinematics of the imaging transducer and the treatment transducer can be different from that mentioned in
It is also clear that the probe is not limited to the preferred use of treatment of the thyroid; it can also be used for the treatment of other organs, such as for example tumors in the neck region, breast tumors, bone tumors or any other organ or tissue anomaly accessible to ultrasound by extracorporeal route. The firing parameters provided in the table can be modified, depending on the organ to be treated, the therapeutic effect sought, transducer characteristics etc.
Specific embodiments of a treatment probe for focused ultrasound according to the present invention have been described for the purpose of illustrating the manner in which the invention may be made and used. It should be understood that implementation of other variations and modifications of the invention and its various aspects will be apparent to those skilled in the art, and that the invention is not limited by the specific embodiments described. It is therefore contemplated to cover by the present invention any and all modifications, variations, or equivalents that fall within the true spirit and scope of the basic underlying principles disclosed and claimed herein.
Number | Date | Country | Kind |
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01 09370 | Jul 2001 | FR | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/FR02/02367 | 7/5/2002 | WO | 00 | 8/5/2004 |
Publishing Document | Publishing Date | Country | Kind |
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WO03/008041 | 1/30/2003 | WO | A |
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